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1-Propanone, 3,3-diphenyl-1-(2,4,6-trimethylphenyl)- is a complex organic compound with the molecular formula C21H22O. It is a derivative of propanone, also known as acetone, with two phenyl groups attached to the carbonyl carbon and a 2,4,6-trimethylphenyl group attached to the terminal carbon. 1-Propanone,3,3-diphenyl-1-(2,4,6-trimethylphenyl)- is characterized by its unique structure, which features a ketone functional group and multiple aromatic rings. It is likely to be used in various chemical reactions and synthesis processes due to its specific functional groups and structural features. The compound's properties, such as solubility, reactivity, and stability, are influenced by the presence of these functional groups and the overall molecular structure.

55800-31-2

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55800-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55800-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,0 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55800-31:
(7*5)+(6*5)+(5*8)+(4*0)+(3*0)+(2*3)+(1*1)=112
112 % 10 = 2
So 55800-31-2 is a valid CAS Registry Number.

55800-31-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-diphenylpropionylmesitylene

1.2 Other means of identification

Product number -
Other names 2.4.6-Trimethyl-β.β-diphenyl-propiophenon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55800-31-2 SDS

55800-31-2Relevant academic research and scientific papers

Iron-Catalyzed α-Alkylation of Ketones with Secondary Alcohols: Access to β-Disubstituted Carbonyl Compounds

Bettoni, Léo,Gaillard, Sylvain,Renaud, Jean-Luc

supporting information, (2020/03/13)

An iron-catalyzed borrowing hydrogen strategy has been applied in the synthesis of β-branched carbonyl compounds. Various secondary benzylic and aliphatic alcohols have been used as alkylating reagents under mild reaction conditions. The ketones have been

CONJUGATE ADDITION OF GRIGNARD REAGENTS TO UNSATURATED KETONES: GC/MS-HPLC STUDY. ISOLATION AND OXIDATION OF E AND Z ENOLS OF A KETONE

Pinkus, A. G.,Logaraj, S.

, p. 6801 - 6806 (2007/10/02)

The conjugate addition of phenylmagnesium bromide to benzalacetomesitylene (1) was studied.The only product resulting from 1,4-addition was Kohler's ketone (4) in 84+/-1 percent yield based on (1) by isolation and analysis.The byproducts from 4 were forme

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